Scientific publications

Publications

• 2016

  • Comments on: fold change rank ordering statistics: a new method for detecting differentially expressed genes

    • Doulaye Dembele
    • Philippe Kastner

    BMC Bioinformatics ; Volume: 17

    HAL DOI

  • SUV4-20 activity in the preimplantation mouse embryo controls timely replication

    • André Eid
    • Diego Rodriguez-Terrones
    • Adam Burton
    • Maria-Elena Torres-Padilla

    Genes and Development ; Volume: 30 ; Page: 2513-2526

    HAL DOI

  • Paternal age effects on sperm FOXK1 and KCNA7 methylation and transmission into the next generation

    • S. Atsem
    • J. Reichenbach
    • R. Potabattula
    • M. Dittrich
    • C. Nava
    • Christel Depienne
    • L. Bohm
    • S. Rost
    • T. Hahn
    • M. Schorsch
    • T. Haaf
    • N. El Hajj

    Human Molecular Genetics ; Volume: 25 ; Page: 4996-5005

    HAL DOI

  • Epidermal-specific deletion of CD44 reveals a function in keratinocytes in response to mechanical stress

    • M. Shatirishvili
    • A. S. Burk
    • C. M. Franz
    • G. Pace
    • T. Kastilan
    • K. Breuhahn
    • E. Hinterseer
    • Andree Dierich
    • L. Bakiri
    • E. F. Wagner
    • H. Ponta
    • T. N. Hartmann
    • M. Tanaka
    • V. Orian-Rousseau

    Cell Death and Disease ; Volume: 7

    HAL DOI

  • Reconstruction of gene regulatory networks defining the cell fate transition processes, Reconstruction des réseaux de régulation géniques responsables du destin cellulaire

    • Valeriya Malysheva

    HAL

  • Lysosomal degradation of insulin granules promotes β-cell failure in type 2 diabetes, La dégradation lysosomale des granules d’insuline favorise l’échec des cellules béta lors d’un diabète de type 2

    • Adrien Pasquier

    HAL

  • Structural studies of protein arginine methyltransferase 2 reveal its interactions with potential substrates and inhibitors

    • Vincent Cura
    • Nils Marechal
    • Nathalie Troffer‐Charlier
    • Jean‐Marc Strub
    • Matthijs J. Haren
    • Nathaniel I. Martin
    • Sarah Cianférani
    • Luc Bonnefond
    • Jean Cavarelli

    Wiley ; Volume: 284 ; Page: 77-96

    DOI

  • Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion

    • Nasim Vasli
    • Elizabeth Harris
    • Jason Karamchandani
    • Eric Bareke
    • Jacek Majewski
    • Norma B. Romero
    • Tanya Stojkovic
    • Rita Barresi
    • Hichem Tasfaout
    • Richard Charlton
    • Edoardo Malfatti
    • Johann Böhm
    • Chiara Marini-Bettolo
    • Karine Choquet
    • Marie-Josée Dicaire
    • Yi-Hong Shao
    • Ana Topf
    • Erin O’ferrall
    • Bruno Eymard
    • Volker Straub
    • ...

    Brain - A Journal of Neurology ; Volume: 140 ; Page: 37-48

    HAL DOI

  • ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

    • C. Mignot
    • M. L. Moutard
    • A. Rastetter
    • L. Boutaud
    • S. Heide
    • T. Billette
    • D. Doummar
    • C. Garel
    • A. Afenjar
    • A. Jacquette
    • D. Lacombe
    • A. Verloes
    • C. Bole-Feysot
    • P. Nitschke
    • C. Masson
    • A. Faudet
    • F. Lesne
    • T. Bienvenu
    • C. Alby
    • T. Attie-Bitach
    • ...

    Brain - A Journal of Neurology ; Volume: 139

    HAL DOI

  • Fragile X syndrome: Are signaling lipids the missing culprits?

    • Ricardos Tabet
    • Nicolas Vitale
    • Hervé Moine

    Biochimie ; Volume: 130 ; Page: 188-194

    HAL DOI